US6121339A - Cationically polymerizable epoxy resins and optical information recording medium made therefrom - Google Patents
Cationically polymerizable epoxy resins and optical information recording medium made therefrom Download PDFInfo
- Publication number
- US6121339A US6121339A US08/952,228 US95222898A US6121339A US 6121339 A US6121339 A US 6121339A US 95222898 A US95222898 A US 95222898A US 6121339 A US6121339 A US 6121339A
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- United States
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- epoxy resin
- resin composition
- adhesive layer
- weight
- information recording
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- Expired - Lifetime
Links
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 100
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 100
- 230000003287 optical effect Effects 0.000 title claims description 48
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 50
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 30
- 238000010538 cationic polymerization reaction Methods 0.000 claims abstract description 18
- 229930185605 Bisphenol Natural products 0.000 claims abstract description 17
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 11
- 239000012790 adhesive layer Substances 0.000 claims description 49
- 230000001070 adhesive effect Effects 0.000 claims description 28
- 239000010410 layer Substances 0.000 claims description 28
- 239000000758 substrate Substances 0.000 claims description 24
- 239000000853 adhesive Substances 0.000 claims description 11
- 239000000945 filler Substances 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 abstract description 3
- 230000000977 initiatory effect Effects 0.000 abstract description 3
- 238000009472 formulation Methods 0.000 abstract description 2
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 239000000126 substance Substances 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 150000002500 ions Chemical class 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000010521 absorption reaction Methods 0.000 description 9
- 230000008859 change Effects 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 125000002091 cationic group Chemical group 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- 230000007797 corrosion Effects 0.000 description 7
- 239000011342 resin composition Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- -1 aromatic diazonium salts Chemical class 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000011241 protective layer Substances 0.000 description 4
- 238000005452 bending Methods 0.000 description 3
- 239000013065 commercial product Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000007650 screen-printing Methods 0.000 description 3
- 230000002411 adverse Effects 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004964 aerogel Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
Images
Classifications
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/256—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers improving adhesion between layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3218—Carbocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/38—Epoxy compounds containing three or more epoxy groups together with di-epoxy compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/253—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
- G11B7/2533—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/258—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of reflective layers
- G11B7/2585—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of reflective layers based on aluminium
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/21—Circular sheet or circular blank
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
Definitions
- the present invention relates to an epoxy resin composition initiating cationic polymerization upon irradiation with energy rays as well as an optical information recording medium such as an optical disk etc. using the resin composition as an adhesive layer.
- optical disks particularly a digital video disk (DVD) that records a moving image and a sound in a digital system.
- DVD digital video disk
- the optical disk e.g. a DVD requiring a large capacity has a structure so-called as a lamination type optical disk which includes, as shown in a schematic view of an optical disk 30 in FIG. 2, two disk substrates 24 having two transparent plastic substrates 21, each being formed on its one side with a recording and reflective layer 22 having formed with a concave and a convex (pits) corresponding to recording information and a protective layer 23 successively in this order, the disk substrates facing each other such that their recording layers (reflective layers) 22 are arranged inside and integrated via an adhesive layer 25.
- a lamination type optical disk which includes, as shown in a schematic view of an optical disk 30 in FIG. 2, two disk substrates 24 having two transparent plastic substrates 21, each being formed on its one side with a recording and reflective layer 22 having formed with a concave and a convex (pits) corresponding to recording information and a protective layer 23 successively in this order, the disk substrates facing each other such that their recording layers (reflective layers) 22 are
- Adhesives such as a hot-melt type adhesive or a radical polymerizable ultraviolet-curing adhesive have been used as the adhesive layer 25 for bonding the disk substrates 24, but they do not suffice for practical purposes in respect of thermal resistance and disk base warpage.
- an optical disk is proposed as described in e.g. Japanese laid-open Publication No. 7-126577 in which a liquid cationic polymerizable, ultraviolet ray-curing adhesive layer is formed on a bonding face between 2 disks, irradiated with energy rays to effect the bonding and then two disks are bonded with pressure, followed by solidification of the layer.
- Such a cationic polymerizable, ultraviolet-curing adhesive layer will initiate curing reaction whether in the air or in a dark place upon exposure to ultraviolet rays once and hence it is expected to have an significant effect on the improvement of the manufacturing process.
- the cationic polymerizable, ultraviolet-curing adhesive has the advantage of less warpage of disk substrates by virtue of less shrinkage at the time of the reaction, and the adhesive layer after curing becomes extremely hard.
- the laminated disk for a DVD is soft and thus tends to easily undergo warpage or bending because it is thinner than a conventional laminated disk such as a laser disk etc.
- the adhesive layer generally requires thermal resistance.
- thermal resistance is improved, the hardness of the adhesive layer is increased while its adhesiveness is lowered in many cases.
- moisture absorption property of the adhesive layer is high, the adhesive layer is easily swollen to lower adhesiveness.
- the present invention was made in view of the above-described problem, and a first object of the present invention is to provide a resin composition excellent in thermal resistance.
- a second object of the present invention is to provide an epoxy resin composition with adhesive properties which are not lowered even if the adhesive layer has increased thermal resistance and hardness or is placed under high humidity.
- a third object of the present invention is to provide an epoxy resin composition for preventing an adhered body from being subject to the adverse effect by an ionic substance in the adhesive layer even under high humidity circumstance.
- a fourth object of the present invention is to provide an optical information recording medium e.g. optical disk excellent in reproduction of recorded signals, which is prepared by bonding disk substrates through an adhesive layer consisting of the resin composition as the first to third objects.
- the present invention is a ultraviolet-curing resin composition, which is an epoxy resin composition initiating cationic polymerization upon exposure to energy rays, comprising at least bisphenol type epoxy resin (A) as an active ingredient, epoxy resin (B) shown in the following formula and cationic polymerization catalyst (C).
- A bisphenol type epoxy resin
- B epoxy resin
- C cationic polymerization catalyst
- R is C n H 2n+1 C(CH 2 ) 3
- a+b+c is 15 in average.
- the epoxy resin composition according to the present invention is one in which the ratio by weight between the bisphenol type epoxy resin (A) in the above epoxy resin composition and the epoxy resin (B) ranges from 100/5 to 100/50.
- the epoxy resin composition according to the present invention is one in which ion exchanger (D) is further incorporated in the above epoxy resin composition.
- An optical information recording medium having a recording layer and an adhesive layer between at least 2 substrates is characterized in that the adhesive layer is formed of an adhesive made of the above-mentioned epoxy resin composition.
- the thermal resistance of the epoxy resin composition undergoing cationic polymerization can be improved by further incorporating the epoxy resin of the above formula into the bisphenol type epoxy resin as the active ingredient.
- both the thermal resistance and adhesive properties of the adhesive layer or the adhesive properties of the adhesive layer under high humidity can be made compatible by mixing the bisphenol type epoxy resin and the epoxy resin of the above formula at a specific weight ratio.
- the recording layer can be prevented from corroding by further incorporating an ion exchanger into the above epoxy resin composition according to the present invention because the ion exchanger captures the ionic substance in the adhesive layer.
- FIG. 1 is a schematic sectional view of an optical information recording medium to which an epoxy resin composition of the present invention is to be applied;
- FIG. 2 is a schematic sectional view of an optical information recording medium.
- An epoxy resin composition of the present invention comprises at least a bisphenol type epoxy resin (A), an epoxy resin (B) shown in the following formula and a cationic polymerization catalyst (C). ##STR3##
- the bisphenol type epoxy resin (A) refers, for example, to bisphenol A type epoxy resin, bisphenol F type epoxy resin etc. obtained by reacting bisphenol A, bisphenol F etc. with epichlorohydrin, or to epoxy resin prepared by hydrogenation thereof.
- the above-mentioned epoxy resin may have been modified with nitrile rubber, urethane etc. when no problem.
- the epoxy resin composition of the present invention is formed as an adhesive layer on a disk substrate, since a technique such as a spin coating, a screen printing or the like is used, the bisphenol type epoxy resin (A), which is incorporated in a large amount, is preferably used in the form of a liquid so as to improve its coating property.
- the bisphenol type epoxy resin (A) is also commercially available. Examples include KRM-2408 (produced by Asahi Denka Kogyo (K.K.)), ST3000 (produced by Toto Kasei (K.K.)) etc.
- the epoxy resin of the above formula used in the present invention is used to improve both the thermal resistance and adhesive properties of the cured resin after irradiation of energy rays.
- the above-mentioned epoxy resin may be synthesized or can be obtained as commercial products such as EHPE-3150 (produced by Daicel Chemical Industries, (Ltd.)) etc.
- This commercial product, EHPE-3150 is the epoxy resin of the above formula where n is 2.
- the ratio by weight between the bisphenol type epoxy resin (A) and the epoxy resin (B) in the epoxy resin composition is preferably in the range of 100/5 to 100/50. With this range given, the thermal resistance and adhesive properties of the cured resin after irradiation of energy rays are well balanced.
- the cationic polymerizable catalyst (C) used in the present invention Upon irradiation with energy rays, the cationic polymerizable catalyst (C) used in the present invention generates so-called Lewis acid and is not particularly limited, and any of such known catalysts can be used. Examples are aromatic diazonium salts, aromatic sulfonium salts, aromatic iodonium salts, aromatic selenium salts etc.
- the cationic polymerizable catalyst (C) can also be obtained as a commercial product.
- aromatic sulfonium salts include SP-150 and SP170 (produced by Asahi Denka Kogyo (K.K.)), UVE1014 (produced by General Electric Co., Ltd.) and FC-509 (manufactured by Minnesota Mining and Manufacturing Co.), and examples of such aromatic diazonium salts include PP-30 (produced by Asahi Denka Kogyo (K.K.)) etc.
- the amount of cationic polymerizable catalyst (C) added is preferably in the range of 1 to 6 parts by weight relative to 100 parts in total of the bisphenol type epoxy resin (A) and the epoxy resin (B).
- the ion exchanger (D) is used to capture ionic substances extracted with water from the cationic polymerization catalyst and bisphenol type epoxy resin.
- the ion exchanger (D) is not particularly limited, and any known one can be used or obtained as a commercial product. Examples include IXE-600, 633, 1100, 1320 (produced by Toagosei Chemical Industry Co., (Ltd.)), Kyoward 500, 600 (produced by Kyowa Kagaku (K.K.)), Tomix AD500, 600 (produced by Tomita Seiyaku (K.K.)), and Ahbanlite CG120 (produced by Organo (Co., Ltd.)).
- the structure of IXE-600 is:
- the amount of ion exchanger (D) added to the epoxy resin composition depends on the type of cationic polymerization catalyst (C) but in general is preferably in the range of 2 to 8 parts by weight relative to 1 part by weight of cationic polymerization catalyst (C).
- Fillers (E) are added as an extender to the adhesive layer or to confer constitutional viscosity on it.
- Aerogel #130, #200, #380, and R974 all of which are fine powder silica) etc. can be used.
- the coupling agent (F) is added to improve the dispersibility of the ion exchanger (D) and the fillers (E).
- the respective components for the epoxy resin composition are mixed uniformly by a dispersing machine such as a three-roll mill etc., and the target epoxy resin composition can be obtained.
- the epoxy resin composition of the present invention can be applied as an adhesive layer onto the bonding faces of disk substrates to produce an optical information recording medium of good qualities being free of distortion or warpage or bending even under the circumstances of high temperature and high humidity.
- an optical information recording medium e.g. an optical disk to which the epoxy resin composition of the present invention has been applied as an adhesive layer is shown in FIG. 1.
- the optical disk 10 is formed of a so-called lamination type optical disk in which two disk substrates 4 having two transparent plastic substrates 1, each being provided on one side with a disk of 0.6 mm in thickness having a recording layer (reflective layer) 2 consisting of e.g. an Al layer etc.
- This optical disk 10 is applied preferably to e.g. the above-mentioned DVD etc.
- an adhesive layer 5 is applied and formed using techniques such as a spin coating method, a screen printing method etc. in which the epoxy resin composition is fed to the bonding faces by means of a dispenser etc. followed by rotation of the disk base 4 to give a uniform thickness, but any other methods can also be used for formation of the adhesive layer 5.
- the thickness of the adhesive layer 5 formed on the bonding faces is generally in the range of 10 to 60 ⁇ m.
- the adhesive layer 5 may be formed on both of disk substrates 4 to be bonded or alternatively it may be formed on only one of disk substrates 4.
- the adhesive layer using the epoxy resin composition of the present invention After formation of the adhesive layer using the epoxy resin composition of the present invention on the bonding faces, it is irradiated with energy rays such as an ultraviolet ray or the like to initiate cationic polymerization.
- energy rays such as an ultraviolet ray or the like
- an ultraviolet ray is used as the energy rays, its irradiation amount is preferably set to be 50 to 1000 mJ/cm 2 .
- the disk substrates 4 After irradiation with the energy rays, the disk substrates 4 are bonded mutually with pressure such that the recording layers 2 are inside, and the desired optical information recording medium 10 can be obtained when the subsequent curing reaction has been completed.
- the following components were thermally molten and mixed with a three-roll mill to obtain a desired epoxy resin composition.
- the epoxy resin composition produced under the above item was used to form the adhesive layer 5 by a screen printing method on each of the bonding faces of 2 disk substrates.
- optical disk optical information recording medium
- the above resin composition was formed into an epoxy resin composition in the same manner as in Embodiment 1, and it was used for preparing an optical disk 10.
- the above resin composition was formed into an epoxy resin composition in the similar manner to that in Embodiment 1, and it was used for preparing an optical disk 10.
- (B') ST5100 is a mixture (produced by Toto Kasei (K.K.)) of solid bisphenol A type epoxy resin and solid hydrogenated bisphenol A type epoxy resin.
- the above resin composition was formed into an epoxy resin composition in the similar manner to that in Embodiment 1, and it was used for preparing an optical disk 10.
- optical disks 10 prepared above in Embodiments 1 to 6 and Comparative Examples 1 to 3 were evaluated with respect to the following evaluation items (a) to (e). The evaluation results are shown in Table 1.
- the epoxy resin composition was applied to 2 plates of glass to give an adhesive area of 25 mm width ⁇ 12.5 mm lap, and it was irradiated with 3 J/cm 2 ultraviolet ray.
- the resulting glass base was used as a sample to be evaluated.
- the prepared disk 10 was stored for 100 hours in a thermostatic chamber at 80° C. and 85% humidity and then examined for external appearance.
- Table 1 the symbol ⁇ is assigned to a sample with a good external appearance without pin holes in the recording layer; ⁇ , a sample with a few pin holes in the recording layer; and X, a sample with innumerable pin holes in the recording layer.
- the prepared disk 10 was stored for 100 hours in a thermostatic chamber at 80° C. and 85% humidity, then taken out, and examined 5 minutes later for tilt angle.
- O is assigned to a sample having a tilt angle of less than 3 mrad
- ⁇ a sample having a tilt angle of from 3 mrad to 5 mrad
- X a sample having a tilt angle of 5 mrad or more.
- tilt angle is most important, and the degrees of distortion and warpage of the optical disk substrate can be directly known. These distortion and warpage are assumed to result from the thermal resistance, adhesive properties and moisture absorption of the adhesive layer.
- the sample (adhesive cured product) was cut into pieces of 0.3 ⁇ 50 ⁇ 50 mm in size and immersed in an organic solvent or acetone for 7 days and examined for change in weight.
- Table 1 the symbol O is assigned to a sample with a change in weight of less than 15 %; ⁇ , a sample with a change in weight of less than 17%; ⁇ , a sample with a change in weight of less than 20%; and X, a sample with a change in weight of 20% or more.
- the adhesive properties of the adhesive layer can be inferred. Because an adhesive layer excellent in adhesiveness has already been sufficiently cured, it may swell in acetone but does not dissolve in it. However, if the adhesive properties of the adhesive layer are insufficient, acetone permeates through that part into the layer to cause swelling and increase the weight of the layer, so that the adhesive properties can be indirectly known.
- the adhesive cured product was cut into pieces of 0.3 ⁇ 50 ⁇ 50 mm in size and immersed in distilled water at 23° C. for 24 hours and examined for change in weight.
- Table 1 the symbol ⁇ is assigned to a sample with a change in weight of less than 5%; and X, a sample with a change in weight of 5% or more.
- the moisture absorption of the adhesive layer can be inferred. That is, the adhesive properties of the adhesive layer under high humidity is indirectly evaluated assuming that the adhesive layer easily absorbing water will drop its adhesive properties under high humidity.
- the water absorption rate and (b) the tilt angle, or the water absorption rate and (e) pressure cooker test described below, are related to each other.
- ⁇ is assigned to a sample with the glass broken without a trace of penetrated water
- ⁇ a sample with the glass broken with a small trace of penetrated water
- X a sample from which the adhesive layer was peeled off without breaking the glass.
- Embodiments 1 to 6 show good results with respect to corrosion properties of disk, tilt angle, thermal resistance, solvent resistance, water absorptivity and pressure cooker test.
- the detailed examination of the results indicate that as the amount of the epoxy resin shown in the above formula is increased, glass transition temperature is raised and thermal resistance is improved, while solvent resistance and adhesive properties in the pressure cooker test tend to be lowered.
- the ratio by weight between the bisphenol type epoxy resin (A) and the epoxy resin (B) of the above formula should be 100/5 to 100/50, preferably 100/10 to 100/40, more preferably 100/15 to 100/25.
- Comparative Example 1 the epoxy resin of the above formula is not incorporated. In this case, the results of the tilt angle, solvent resistance and pressure cooker test are not good.
- Comparative Example 2 the solid bisphenol type epoxy resin has been incorporated in place of the epoxy resin of the above formula. In this case, the results of the tilt angle, solvent resistance and pressure cooker test are not good similarly to comparative Example 1.
- Comparative Example 3 the alicyclic epoxy resin (A') has been incorporated in place of the bisphenol type epoxy resin. In this case, moisture absorptivity is high, and simultaneously the results of the pressure cooker test and tilt angle are not good.
- the epoxy resin composition of the present invention can be applied as an adhesive layer to an optical disk to construct an optical information recording medium of good qualities which is excellent in thermal resistance, solvent resistance and moisture resistance and does not cause the distortion and warpage under the circumstances of high temperature and high humidity.
- Embodiments as illustrated above are related to optical information recording media where the recording layer 2 and the protective layer 3 have been sequentially formed in this order on the plastic substrate 1 to form the disk substrate 4.
- optical information recording media can be obtained similarly by applying the epoxy resin composition of the present invention as the adhesive layer 5.
- the epoxy resin composition of the present invention and the optical information recording media using the same are not limited to the examples illustrated above and there can be effected various modifications within the spirit of the present invention.
- the epoxy resin composition of the present invention initiates reaction upon irradiation with energy rays and gives a product excellent in thermal resistance and adhesive properties, and the adhesive properties thereof are not lowered even under the circumstances of high humidity.
- the corrosion of the recording layer due to ionic substances in the adhesive layer is prevented by applying the epoxy resin composition of the present invention as an adhesive layer to optical information recording media such as an optical disk. Further, the optical information recording media do not distort and warpage, and thus optical recording media excellent in reproduction characteristic of recording signals can be obtained.
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Abstract
An epoxy resin composition according to the present invention is one initiating cationic polymerization upon irradiation with energy rays. The epoxy resin composition is formed of at least bisphenol epoxy resin (A) as an active ingredient, epoxy resin (B) shown in the following formula and cationic polymerization catalyst (C). ##STR1##
Description
The present invention relates to an epoxy resin composition initiating cationic polymerization upon irradiation with energy rays as well as an optical information recording medium such as an optical disk etc. using the resin composition as an adhesive layer.
Recently, attention is drawn to optical disks, particularly a digital video disk (DVD) that records a moving image and a sound in a digital system.
Generally, the optical disk e.g. a DVD requiring a large capacity has a structure so-called as a lamination type optical disk which includes, as shown in a schematic view of an optical disk 30 in FIG. 2, two disk substrates 24 having two transparent plastic substrates 21, each being formed on its one side with a recording and reflective layer 22 having formed with a concave and a convex (pits) corresponding to recording information and a protective layer 23 successively in this order, the disk substrates facing each other such that their recording layers (reflective layers) 22 are arranged inside and integrated via an adhesive layer 25.
Adhesives such as a hot-melt type adhesive or a radical polymerizable ultraviolet-curing adhesive have been used as the adhesive layer 25 for bonding the disk substrates 24, but they do not suffice for practical purposes in respect of thermal resistance and disk base warpage.
Under the circumstances, a method of manufacturing an optical disk is proposed as described in e.g. Japanese laid-open Publication No. 7-126577 in which a liquid cationic polymerizable, ultraviolet ray-curing adhesive layer is formed on a bonding face between 2 disks, irradiated with energy rays to effect the bonding and then two disks are bonded with pressure, followed by solidification of the layer.
Such a cationic polymerizable, ultraviolet-curing adhesive layer will initiate curing reaction whether in the air or in a dark place upon exposure to ultraviolet rays once and hence it is expected to have an significant effect on the improvement of the manufacturing process. The cationic polymerizable, ultraviolet-curing adhesive has the advantage of less warpage of disk substrates by virtue of less shrinkage at the time of the reaction, and the adhesive layer after curing becomes extremely hard.
However, even in cases where such cationic polymerizable, ultraviolet-curing adhesives are used, the resulting products cannot suffice under the circumstances of high temperature and high humidity.
For example, if the above-mentioned optical disk is stored under the circumstances of high temperature and high humidity, a tilt angle (i.e. angle from a horizontal plane) of the optical disk is enlarged due to distortion or warpage of the disk, causing an adverse effect on the reproduction of a recorded signal so that the recorded information cannot correctly be read out.
This is particularly a great problem for a DVD requiring high reading accuracy because a concave and a convex (pits) on the recording layer have been further minimized for large capacity.
Further, the laminated disk for a DVD is soft and thus tends to easily undergo warpage or bending because it is thinner than a conventional laminated disk such as a laser disk etc.
Furthermore, in the recording layer there occurs a trace of corrosion under the circumstances of high temperature and high humidity.
As a result of detailed examinations by the present inventors et al., it was estimated that the warpage or bending under the circumstances of high temperature and high humidity resulted from the inadequate thermal resistance and adhesiveness of the adhesive layer.
That is, under the circumstances of high temperature and high humidity, the adhesive layer generally requires thermal resistance. However, if thermal resistance is improved, the hardness of the adhesive layer is increased while its adhesiveness is lowered in many cases. In addition, if the moisture absorption property of the adhesive layer is high, the adhesive layer is easily swollen to lower adhesiveness. These reasons presumably cause the above distortion or warpage.
For the corrosion of the recording layer, it is estimated that because cationic polymerization makes use of an organic salt as a catalyst, such an ionic substance remaining in the adhesive layer causes the corrosion of a metal in an Al layer etc. forming the recording layer at high temperature and high humidity.
The present invention was made in view of the above-described problem, and a first object of the present invention is to provide a resin composition excellent in thermal resistance.
Further, a second object of the present invention is to provide an epoxy resin composition with adhesive properties which are not lowered even if the adhesive layer has increased thermal resistance and hardness or is placed under high humidity.
Moreover, a third object of the present invention is to provide an epoxy resin composition for preventing an adhered body from being subject to the adverse effect by an ionic substance in the adhesive layer even under high humidity circumstance.
Finally, a fourth object of the present invention is to provide an optical information recording medium e.g. optical disk excellent in reproduction of recorded signals, which is prepared by bonding disk substrates through an adhesive layer consisting of the resin composition as the first to third objects.
The present invention is a ultraviolet-curing resin composition, which is an epoxy resin composition initiating cationic polymerization upon exposure to energy rays, comprising at least bisphenol type epoxy resin (A) as an active ingredient, epoxy resin (B) shown in the following formula and cationic polymerization catalyst (C). In the following formula, R is Cn H2n+1 C(CH2)3, and a+b+c is 15 in average. ##STR2##
The epoxy resin composition according to the present invention is one in which the ratio by weight between the bisphenol type epoxy resin (A) in the above epoxy resin composition and the epoxy resin (B) ranges from 100/5 to 100/50.
The epoxy resin composition according to the present invention is one in which ion exchanger (D) is further incorporated in the above epoxy resin composition.
An optical information recording medium according to the present invention having a recording layer and an adhesive layer between at least 2 substrates is characterized in that the adhesive layer is formed of an adhesive made of the above-mentioned epoxy resin composition.
In the present invention, the thermal resistance of the epoxy resin composition undergoing cationic polymerization can be improved by further incorporating the epoxy resin of the above formula into the bisphenol type epoxy resin as the active ingredient.
Further, both the thermal resistance and adhesive properties of the adhesive layer or the adhesive properties of the adhesive layer under high humidity can be made compatible by mixing the bisphenol type epoxy resin and the epoxy resin of the above formula at a specific weight ratio.
Further, the recording layer can be prevented from corroding by further incorporating an ion exchanger into the above epoxy resin composition according to the present invention because the ion exchanger captures the ionic substance in the adhesive layer.
Further, no distortion or warpage occurs even under the circumstances of high temperature and high humidity by using the adhesive composition as an adhesive layer on the bonding face of disk substrates according to the present invention, and therefore, an optical information recording medium excellent in reproducing a recorded signal can be obtained.
FIG. 1 is a schematic sectional view of an optical information recording medium to which an epoxy resin composition of the present invention is to be applied; and
FIG. 2 is a schematic sectional view of an optical information recording medium.
An epoxy resin composition of the present invention comprises at least a bisphenol type epoxy resin (A), an epoxy resin (B) shown in the following formula and a cationic polymerization catalyst (C). ##STR3##
In the present invention, the bisphenol type epoxy resin (A) refers, for example, to bisphenol A type epoxy resin, bisphenol F type epoxy resin etc. obtained by reacting bisphenol A, bisphenol F etc. with epichlorohydrin, or to epoxy resin prepared by hydrogenation thereof.
The above-mentioned epoxy resin may have been modified with nitrile rubber, urethane etc. when no problem.
Meanwhile, if the epoxy resin composition of the present invention is formed as an adhesive layer on a disk substrate, since a technique such as a spin coating, a screen printing or the like is used, the bisphenol type epoxy resin (A), which is incorporated in a large amount, is preferably used in the form of a liquid so as to improve its coating property.
The bisphenol type epoxy resin (A) is also commercially available. Examples include KRM-2408 (produced by Asahi Denka Kogyo (K.K.)), ST3000 (produced by Toto Kasei (K.K.)) etc.
The epoxy resin of the above formula used in the present invention is used to improve both the thermal resistance and adhesive properties of the cured resin after irradiation of energy rays.
The above-mentioned epoxy resin may be synthesized or can be obtained as commercial products such as EHPE-3150 (produced by Daicel Chemical Industries, (Ltd.)) etc. This commercial product, EHPE-3150, is the epoxy resin of the above formula where n is 2.
The ratio by weight between the bisphenol type epoxy resin (A) and the epoxy resin (B) in the epoxy resin composition is preferably in the range of 100/5 to 100/50. With this range given, the thermal resistance and adhesive properties of the cured resin after irradiation of energy rays are well balanced.
In the above weight ratio, a small amount of the epoxy resin (B) results in a decrease in the improving effect on thermal resistance. On the other hand, a large amount of the epoxy resin (B) leads in many cases to an increase in the hardness and an decrease in the adhesive properties of the cured resin.
Upon irradiation with energy rays, the cationic polymerizable catalyst (C) used in the present invention generates so-called Lewis acid and is not particularly limited, and any of such known catalysts can be used. Examples are aromatic diazonium salts, aromatic sulfonium salts, aromatic iodonium salts, aromatic selenium salts etc.
The cationic polymerizable catalyst (C) can also be obtained as a commercial product. Examples of such aromatic sulfonium salts include SP-150 and SP170 (produced by Asahi Denka Kogyo (K.K.)), UVE1014 (produced by General Electric Co., Ltd.) and FC-509 (manufactured by Minnesota Mining and Manufacturing Co.), and examples of such aromatic diazonium salts include PP-30 (produced by Asahi Denka Kogyo (K.K.)) etc.
The amount of cationic polymerizable catalyst (C) added is preferably in the range of 1 to 6 parts by weight relative to 100 parts in total of the bisphenol type epoxy resin (A) and the epoxy resin (B).
Other components such as ion exchanger (D), fillers (E) and coupling agent (F) can be added to the epoxy resin composition of the present invention.
The ion exchanger (D) is used to capture ionic substances extracted with water from the cationic polymerization catalyst and bisphenol type epoxy resin. The ion exchanger (D) is not particularly limited, and any known one can be used or obtained as a commercial product. Examples include IXE-600, 633, 1100, 1320 (produced by Toagosei Chemical Industry Co., (Ltd.)), Kyoward 500, 600 (produced by Kyowa Kagaku (K.K.)), Tomix AD500, 600 (produced by Tomita Seiyaku (K.K.)), and Ahbanlite CG120 (produced by Organo (Co., Ltd.)). The structure of IXE-600 is:
Bi.sub.2 O.sub.3 •Sb.sub.2 O.sub.5 •Bi(NO.sub.3).sub.3.
The amount of ion exchanger (D) added to the epoxy resin composition depends on the type of cationic polymerization catalyst (C) but in general is preferably in the range of 2 to 8 parts by weight relative to 1 part by weight of cationic polymerization catalyst (C).
With an amount of less than 2 parts by weight given, pin holes readily occur in the recording layer, while, with an amount of larger than 8 parts by weight, the hardness of the epoxy resin composition is often low.
Fillers (E) are added as an extender to the adhesive layer or to confer constitutional viscosity on it. For example, Aerogel #130, #200, #380, and R974 (all of which are fine powder silica) etc. can be used.
Also, the coupling agent (F) is added to improve the dispersibility of the ion exchanger (D) and the fillers (E).
The respective components for the epoxy resin composition are mixed uniformly by a dispersing machine such as a three-roll mill etc., and the target epoxy resin composition can be obtained.
Then, the epoxy resin composition of the present invention can be applied as an adhesive layer onto the bonding faces of disk substrates to produce an optical information recording medium of good qualities being free of distortion or warpage or bending even under the circumstances of high temperature and high humidity.
The structure of an optical information recording medium e.g. an optical disk to which the epoxy resin composition of the present invention has been applied as an adhesive layer is shown in FIG. 1. As shown in FIG. 1, the optical disk 10 is formed of a so-called lamination type optical disk in which two disk substrates 4 having two transparent plastic substrates 1, each being provided on one side with a disk of 0.6 mm in thickness having a recording layer (reflective layer) 2 consisting of e.g. an Al layer etc. with a concave and a convex (pits) indicating information and a protective layer 3 of 5 to 10 μm in thickness in this order, are prepared, and the two disk substrates 4 are faced each other such that their recording layers (reflective layers) 2 are arranged inside and integrated via an adhesive layer 5.
This optical disk 10 is applied preferably to e.g. the above-mentioned DVD etc.
To apply the epoxy resin composition of the present invention to the bonding faces of disk substrates 4 in the optical disk 10, it is general that an adhesive layer 5 is applied and formed using techniques such as a spin coating method, a screen printing method etc. in which the epoxy resin composition is fed to the bonding faces by means of a dispenser etc. followed by rotation of the disk base 4 to give a uniform thickness, but any other methods can also be used for formation of the adhesive layer 5.
The thickness of the adhesive layer 5 formed on the bonding faces is generally in the range of 10 to 60 μm.
The adhesive layer 5 may be formed on both of disk substrates 4 to be bonded or alternatively it may be formed on only one of disk substrates 4.
After formation of the adhesive layer using the epoxy resin composition of the present invention on the bonding faces, it is irradiated with energy rays such as an ultraviolet ray or the like to initiate cationic polymerization.
If an ultraviolet ray is used as the energy rays, its irradiation amount is preferably set to be 50 to 1000 mJ/cm2.
After irradiation with the energy rays, the disk substrates 4 are bonded mutually with pressure such that the recording layers 2 are inside, and the desired optical information recording medium 10 can be obtained when the subsequent curing reaction has been completed.
Hereinafter, the epoxy resin composition of the present invention and the optical information recording medium using the same are described in detail for their properties and characteristics with reference to the practical embodiments.
(i) Epoxy Resin Composition
The following components were thermally molten and mixed with a three-roll mill to obtain a desired epoxy resin composition.
(A) Hydrogenated bisphenol A type epoxy resin (KRM2408, produced by Asahi Denka Kogyo (K.K.)) 100 parts by weight
(B) Epoxy resin having the structure of the above formula (EHPE-3150, produced by Daicel Chemical (Industries, Ltd.)) 5 parts by weight
(C) Cationic polymerization catalyst (SP-150, produced by Asahi Denka Kogyo (K.K.)) 5 parts by weight
(D) Ion exchanger (IXE-1320, produced by Toagosei Chemical Industry (Co., Ltd.)) 20 parts by weight
(E) Fine power silica 3 parts by weight
(ii) Manufacturing of Optical Recording medium
The epoxy resin composition produced under the above item was used to form the adhesive layer 5 by a screen printing method on each of the bonding faces of 2 disk substrates.
Then, 100 mJ/cm2 ultraviolet ray was irradiated, and the bonding faces were laminated to obtain the desired optical disk (optical information recording medium) 10 shown in FIG. 1.
(B) The epoxy resin having the structure of the above formula (EHPE-3150, produced by Daicel Chemical Industries, (Ltd.)) was incorporated at ratios of 10, 20, 30, 40 and 50 parts by weight respectively to form epoxy resin compositions in the same manner as in Embodiment 1. The resulting compositions were used to produce optical disks (optical information recording media) 10 of Embodiments 2 to 6, respectively.
(A) Hydrogenated bisphenol A type epoxy resin (KRM2408, produced by Asahi Denka Kogyo (K.K.)) 100 parts by weight
(C) Cationic polymerization catalyst (SP-150, produced by Asahi Denka Kogyo (K.K.)) 5 parts by weight
(D) Ion exchanger (IXE-1320, produced by Toagosei Chemical Industry (Co., Ltd.)) 20 parts by weight
(E) Fine powder silica 3 parts by weight
The above resin composition was formed into an epoxy resin composition in the same manner as in Embodiment 1, and it was used for preparing an optical disk 10.
(A) Hydrogenated bisphenol A type epoxy resin (KRM2408, produced by Asahi Denka Kogyo (K.K.)) 100 parts by weight
(B') Solid bisphenol A type epoxy resin+Hydrogenated bisphenol A type epoxy resin (ST5100, produced by Toto Kasei (K.K.)) 20 parts by weight
(C) Cationic polymerization catalyst (SP-150, produced by Asahi Denka Kogyo (K.K.)) 5 parts by weight
(D) Ion exchanger (IXE-1320, produced by Toagosei Chemical Industry (Co., Ltd.)) 20 parts by weight
(E) Fine powder silica 3 parts by weight
The above resin composition was formed into an epoxy resin composition in the similar manner to that in Embodiment 1, and it was used for preparing an optical disk 10.
In the above ingredients, (B') ST5100 is a mixture (produced by Toto Kasei (K.K.)) of solid bisphenol A type epoxy resin and solid hydrogenated bisphenol A type epoxy resin.
(A') Solid alicyclic epoxy resin (ERL4299) 100 parts by weight
(B) Epoxy resin having the structure of the above formula (EHPE-3150, produced by Daicel Chemical Industries, (Ltd.)) 20 parts by weight
(C) Cationic polymerization catalyst (SP-150, produced by Asahi Denka Kogyo (K.K.)) 5 parts by weight
(D) Ion exchanger (IXE-1320, produced by Toagosei Chemical Industry (Co., Ltd.)) 20 parts by weight
(E) Fine powder silica 3 parts by weight
The above resin composition was formed into an epoxy resin composition in the similar manner to that in Embodiment 1, and it was used for preparing an optical disk 10.
(iii) Evaluation Methods
The optical disks 10 prepared above in Embodiments 1 to 6 and Comparative Examples 1 to 3 were evaluated with respect to the following evaluation items (a) to (e). The evaluation results are shown in Table 1.
TABLE 1
__________________________________________________________________________
Embodiment
Embodiment
Embodiment Embodiment
Embodiment
comparative
comparative
comparative
1 2 3 Embodiment
5 6 example 1
example 2
example 3
__________________________________________________________________________
Ingredients of
Adhesive Layer
KRM2408 100 100 100 100 100 100 100 100 --
(A)
EHPE3150 5 10 20 30 40 50 -- -- 20
(B)
ST5100 -- -- -- -- -- -- -- 20 --
ERL4299 -- -- -- -- -- -- -- -- 100
SP150 5 5 5 5 5 5 5 5 5
(C)
IXE1320 20 20 20 20 20 20 20 20 20
(D)
Fine Powder Silica 3 3 3 3 3 3 3 3 3
(E)
Value
Corrosion Properties ◯ ◯ ◯ .largecir
cle. .largecircle
. ◯
◯
◯
◯
of Disk
Solvent
Resistance
◯
◯
◯
◯
Δ Δ
Δ Δ
◯
Pressure Cooker
◯
◯
◯
◯
Δ Δ
Δ Δ
Δ
Test
Water Absorption ◯ ◯ ◯ ◯
◯
◯
◯
◯ X
Degree
Tilt Angle Δ ◯ ◯ ◯ .largecircl
e. ◯
X X Δ
Glass Transition
80 90 104 123
135 147 75 75
93
Temp. ° C.
__________________________________________________________________________
For the evaluation item (e), the epoxy resin composition was applied to 2 plates of glass to give an adhesive area of 25 mm width×12.5 mm lap, and it was irradiated with 3 J/cm2 ultraviolet ray. The resulting glass base was used as a sample to be evaluated.
(a) corrosion Properties of Disk
The prepared disk 10 was stored for 100 hours in a thermostatic chamber at 80° C. and 85% humidity and then examined for external appearance. In Table 1, the symbol ◯ is assigned to a sample with a good external appearance without pin holes in the recording layer; Δ, a sample with a few pin holes in the recording layer; and X, a sample with innumerable pin holes in the recording layer.
(b) Tilt Angle
The prepared disk 10 was stored for 100 hours in a thermostatic chamber at 80° C. and 85% humidity, then taken out, and examined 5 minutes later for tilt angle. In Table 1, O is assigned to a sample having a tilt angle of less than 3 mrad; ◯, a sample having a tilt angle of from 3 mrad to 5 mrad; and X, a sample having a tilt angle of 5 mrad or more.
This evaluation of tilt angle is most important, and the degrees of distortion and warpage of the optical disk substrate can be directly known. These distortion and warpage are assumed to result from the thermal resistance, adhesive properties and moisture absorption of the adhesive layer.
(c) Solvent Resistance
The sample (adhesive cured product) was cut into pieces of 0.3×50×50 mm in size and immersed in an organic solvent or acetone for 7 days and examined for change in weight. In Table 1, the symbol O is assigned to a sample with a change in weight of less than 15 %; ◯, a sample with a change in weight of less than 17%; Δ, a sample with a change in weight of less than 20%; and X, a sample with a change in weight of 20% or more.
By this evaluation of solvent resistance, the adhesive properties of the adhesive layer can be inferred. Because an adhesive layer excellent in adhesiveness has already been sufficiently cured, it may swell in acetone but does not dissolve in it. However, if the adhesive properties of the adhesive layer are insufficient, acetone permeates through that part into the layer to cause swelling and increase the weight of the layer, so that the adhesive properties can be indirectly known.
(d) Water Absorption Rate
The adhesive cured product was cut into pieces of 0.3×50×50 mm in size and immersed in distilled water at 23° C. for 24 hours and examined for change in weight. In Table 1, the symbol ◯ is assigned to a sample with a change in weight of less than 5%; and X, a sample with a change in weight of 5% or more.
By this evaluation of water absorption rate, the moisture absorption of the adhesive layer can be inferred. That is, the adhesive properties of the adhesive layer under high humidity is indirectly evaluated assuming that the adhesive layer easily absorbing water will drop its adhesive properties under high humidity.
The water absorption rate and (b) the tilt angle, or the water absorption rate and (e) pressure cooker test described below, are related to each other.
(e) Pressure Cooker Test
Glass substrates bonded via the above-described adhesive layer were kept under the conditions of 121° C., 2 atmospheric pressure and 100% relative humidity (RH) for 50 hours in a PC (pressure cooker) machine. Thereafter, the sample was taken out from the PC machine and examined for tensile strength by means of Tension (i.e. tensile strength tester).
In Table 1, the symbol ◯ is assigned to a sample with the glass broken without a trace of penetrated water; Δ, a sample with the glass broken with a small trace of penetrated water; X, a sample from which the adhesive layer was peeled off without breaking the glass.
By this evaluation, the adhesive properties of the as well as the lowering of the adhesive properties of the adhesive layer due to moisture absorption can be known.
In Table 1, Embodiments 1 to 6 show good results with respect to corrosion properties of disk, tilt angle, thermal resistance, solvent resistance, water absorptivity and pressure cooker test. The detailed examination of the results indicate that as the amount of the epoxy resin shown in the above formula is increased, glass transition temperature is raised and thermal resistance is improved, while solvent resistance and adhesive properties in the pressure cooker test tend to be lowered.
Accordingly, it is estimated that the ratio by weight between the bisphenol type epoxy resin (A) and the epoxy resin (B) of the above formula should be 100/5 to 100/50, preferably 100/10 to 100/40, more preferably 100/15 to 100/25.
In Comparative Example 1, the epoxy resin of the above formula is not incorporated. In this case, the results of the tilt angle, solvent resistance and pressure cooker test are not good.
In Comparative Example 2, the solid bisphenol type epoxy resin has been incorporated in place of the epoxy resin of the above formula. In this case, the results of the tilt angle, solvent resistance and pressure cooker test are not good similarly to comparative Example 1.
In Comparative Example 3, the alicyclic epoxy resin (A') has been incorporated in place of the bisphenol type epoxy resin. In this case, moisture absorptivity is high, and simultaneously the results of the pressure cooker test and tilt angle are not good.
As can be seen from the above results, the epoxy resin composition of the present invention can be applied as an adhesive layer to an optical disk to construct an optical information recording medium of good qualities which is excellent in thermal resistance, solvent resistance and moisture resistance and does not cause the distortion and warpage under the circumstances of high temperature and high humidity.
The Embodiments as illustrated above are related to optical information recording media where the recording layer 2 and the protective layer 3 have been sequentially formed in this order on the plastic substrate 1 to form the disk substrate 4. However, even if the disk substrate 4 is designed such that it is formed with other layers in addition to the recording layer 2 and the protective layer 3, optical information recording media can be obtained similarly by applying the epoxy resin composition of the present invention as the adhesive layer 5.
The epoxy resin composition of the present invention and the optical information recording media using the same are not limited to the examples illustrated above and there can be effected various modifications within the spirit of the present invention.
The epoxy resin composition of the present invention as described above initiates reaction upon irradiation with energy rays and gives a product excellent in thermal resistance and adhesive properties, and the adhesive properties thereof are not lowered even under the circumstances of high humidity.
In addition, the corrosion of the recording layer due to ionic substances in the adhesive layer is prevented by applying the epoxy resin composition of the present invention as an adhesive layer to optical information recording media such as an optical disk. Further, the optical information recording media do not distort and warpage, and thus optical recording media excellent in reproduction characteristic of recording signals can be obtained.
Accordingly, it can be applied to a large-capacity optical disk such as a DVD etc. to constitute excellent optical information recording media.
Claims (5)
1. An epoxy resin composition, which initiates cationic polymerization upon irradiation, which consists of:
(A) at least one bisphenol epoxy resin;
(B) at least one epoxy resin of the formula; ##STR4## where R is ##STR5## and (C) a cationic polymerization catalyst;
(D) optionally, ion exchanger; and
(E) optionally, a filler.
2. An epoxy resin composition according to claim 1, wherein a ratio by weight of the bisphenol epoxy resin (A) in said epoxy resin composition and the epoxy resin (B) shown in the above formula ranges from 100/5 to 100/50.
3. In an optical information recording medium having a recording layer and an adhesive layer between at least two substrates, said optical information recording medium being characterized in that said adhesive layer comprises an adhesive made of the epoxy resin composition claimed in claim 1.
4. An epoxy resin composition according to claim 1, wherein the ion exchanger is
Bi.sub.2 O.sub.3 •Sb.sub.2 O.sub.5 •Bi(NO.sub.3).sub.3.
5.
5. The epoxy resin composition according to claim 1, wherein an ion exchanger is present.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP05955596A JP3289125B2 (en) | 1996-03-15 | 1996-03-15 | Optical information recording medium |
| JP8-059555 | 1996-03-15 | ||
| PCT/JP1997/000848 WO1997033932A1 (en) | 1996-03-15 | 1997-03-17 | Epoxy resin composition and optical information recording medium made by using the same |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/591,695 Division US6447867B1 (en) | 1996-03-15 | 2000-06-09 | Epoxy resin composition and optical information recording medium using the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US6121339A true US6121339A (en) | 2000-09-19 |
Family
ID=13116625
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/952,228 Expired - Lifetime US6121339A (en) | 1996-03-15 | 1997-03-17 | Cationically polymerizable epoxy resins and optical information recording medium made therefrom |
| US09/591,695 Expired - Lifetime US6447867B1 (en) | 1996-03-15 | 2000-06-09 | Epoxy resin composition and optical information recording medium using the same |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/591,695 Expired - Lifetime US6447867B1 (en) | 1996-03-15 | 2000-06-09 | Epoxy resin composition and optical information recording medium using the same |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6121339A (en) |
| EP (1) | EP0827974B1 (en) |
| JP (1) | JP3289125B2 (en) |
| KR (1) | KR100482401B1 (en) |
| CN (1) | CN1092680C (en) |
| AU (1) | AU713122B2 (en) |
| CA (1) | CA2220062C (en) |
| DE (1) | DE69706255T2 (en) |
| WO (1) | WO1997033932A1 (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6278683B1 (en) * | 1999-06-10 | 2001-08-21 | Sony Chemicals Corp. | Optical recording medium |
| US20020053397A1 (en) * | 2000-11-06 | 2002-05-09 | Dainippon Ink And Chemicals, Inc. | Method for bonding members, and disc manufacturing method and device |
| US6447867B1 (en) * | 1996-03-15 | 2002-09-10 | Sony Chemicals Corporation | Epoxy resin composition and optical information recording medium using the same |
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Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6447867B1 (en) * | 1996-03-15 | 2002-09-10 | Sony Chemicals Corporation | Epoxy resin composition and optical information recording medium using the same |
| US6537423B1 (en) * | 1999-03-23 | 2003-03-25 | Dainippon Ink And Chemicals, Inc. | Optical disk production device |
| US6278683B1 (en) * | 1999-06-10 | 2001-08-21 | Sony Chemicals Corp. | Optical recording medium |
| US6645595B2 (en) * | 1999-08-23 | 2003-11-11 | Sony Chemicals Corp. | Optical medium |
| US20020053397A1 (en) * | 2000-11-06 | 2002-05-09 | Dainippon Ink And Chemicals, Inc. | Method for bonding members, and disc manufacturing method and device |
| US20060153993A1 (en) * | 2003-07-22 | 2006-07-13 | Helmut Schmidt | Liquid-repellent coating composition and coating having high alkali resistance |
| US20060154091A1 (en) * | 2003-07-22 | 2006-07-13 | Helmut Schmidt | Liquid-repellent, alkali-resistant coating composition and coating suitable for pattern forming |
| US7985477B2 (en) * | 2003-07-22 | 2011-07-26 | Leibniz- Institut Fuer Neue Materialien Gemeinnuetzige GmbH | Liquid-repellent, alkali-resistant coating composition and coating suitable for pattern forming |
| US20080213547A1 (en) * | 2005-01-21 | 2008-09-04 | Carsten Becker-Willinger | Composite Composition for Micropatterned Layers Having High Relaxation Ability, High Chemical Resistance and Mechanical Stability |
| US8535796B2 (en) | 2005-01-21 | 2013-09-17 | Leibniz-Institut Fuer Neue Materialien Gemeinnuetzige Gmbh | Composite composition for micropatterned layers having high relaxation ability, high chemical resistance and mechanical stability |
| US20090258197A1 (en) * | 2006-07-18 | 2009-10-15 | Etsuko Hino | Composite Composition for Micropatterned Layers |
| US20100260978A9 (en) * | 2006-07-18 | 2010-10-14 | Etsuko Hino | Composite Composition for Micropatterned Layers |
| US8680179B2 (en) | 2006-07-18 | 2014-03-25 | Leibniz-Institut Fuer Neue Materialien Gemeinnuetzige Gmbh | Composite composition for micropatterned layers |
| US20110318882A1 (en) * | 2010-06-24 | 2011-12-29 | Xiaoming Wu | Method of restricting chip movement upon bonding to rigid substrate using spray coatable adhesive |
Also Published As
| Publication number | Publication date |
|---|---|
| US6447867B1 (en) | 2002-09-10 |
| EP0827974A1 (en) | 1998-03-11 |
| DE69706255T2 (en) | 2002-04-11 |
| CN1092680C (en) | 2002-10-16 |
| AU1942297A (en) | 1997-10-01 |
| EP0827974A4 (en) | 1999-02-24 |
| CA2220062C (en) | 2003-11-11 |
| EP0827974B1 (en) | 2001-08-22 |
| WO1997033932A1 (en) | 1997-09-18 |
| JPH09249734A (en) | 1997-09-22 |
| DE69706255D1 (en) | 2001-09-27 |
| KR19990014750A (en) | 1999-02-25 |
| JP3289125B2 (en) | 2002-06-04 |
| KR100482401B1 (en) | 2005-11-01 |
| AU713122B2 (en) | 1999-11-25 |
| CN1181766A (en) | 1998-05-13 |
| CA2220062A1 (en) | 1997-09-18 |
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